| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:43656044-43656414 | Rare:63 | ||||
| chrX:43743445-43743711 | Common:1; Rare:26 | ||||
| chrX:46545380-46545524 | Rare:25 | ||||
| chrX:47144474-47144837 | Common:2; Rare:79; Clinvar (benign):1 | ||||
| chrX:47145043-47145311 | Rare:37 | ||||
| chrX:47483169-47483277 | Common:3; Rare:14 | ||||
| chrX:47584744-47585589 | Common:6; Rare:167 | ||||
| chrX:47836791-47836953 | Common:1; Rare:38 | ||||
| chrX:48003929-48004142 | Rare:56 | ||||
| chrX:48475952-48476247 | Rare:52 | ||||
| chrX:48508865-48509028 | Rare:30 | ||||
| chrX:48521590-48521895 | Common:1; Rare:55 | ||||
| chrX:48589894-48590053 | Common:3; Rare:35 | ||||
| chrX:48676336-48676615 | Common:1; Rare:61 | ||||
| chrX:48696584-48696777 | Rare:43 |